WO2012113269A1 - 提高乙二醇产品质量的方法 - Google Patents
提高乙二醇产品质量的方法 Download PDFInfo
- Publication number
- WO2012113269A1 WO2012113269A1 PCT/CN2012/000240 CN2012000240W WO2012113269A1 WO 2012113269 A1 WO2012113269 A1 WO 2012113269A1 CN 2012000240 W CN2012000240 W CN 2012000240W WO 2012113269 A1 WO2012113269 A1 WO 2012113269A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- ethylene glycol
- catalyst
- solid oxide
- bed reactor
- packed bed
- Prior art date
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
- C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
- C07C29/147—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof
- C07C29/149—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof with hydrogen or hydrogen-containing gases
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
- C07C29/88—Separation; Purification; Use of additives, e.g. for stabilisation by treatment giving rise to a chemical modification of at least one compound
- C07C29/90—Separation; Purification; Use of additives, e.g. for stabilisation by treatment giving rise to a chemical modification of at least one compound using hydrogen only
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Definitions
- the present invention relates to a process for improving the quality of ethylene glycol products, and more particularly to a process for improving the quality of oxalates, preferably hydrogenated oxalate or hydrogenated oxalate.
- Ethylene glycol (EG) is an important organic chemical raw material used in the production of polyester fiber, antifreeze, unsaturated polyester resin, lubricant, plasticizer, nonionic surfactant and explosives. It can be used in industries such as paints, photographic developers, brake fluids and inks. It is used as a solvent and medium for ammonium perborate. It is used in the production of special solvent glycol ethers. It is widely used. One of the most important uses is for The basic raw material for the manufacture of polyester (PET) polyester fibers, which is commonly referred to as fiber grade ethylene glycol products.
- PET polyester
- ethylene glycol production at home and abroad mainly adopts an oil route, which is a direct hydration or pressurized water legal process.
- the process is to prepare a mixed aqueous solution of ethylene oxide and water at a ratio of 1:20 to 22 (molar ratio).
- the important factor affecting the ultraviolet light transmittance at 220 nm of the ethylene glycol product is different from the petroleum route.
- the aldehyde-containing by-products are less.
- Other non-aldehyde-based carbonyl compounds may be important factors influencing the UV light transmittance at 220 nm of ethylene glycol products.
- an ion exchange resin is generally used as a catalyst to purify and purify ethylene glycol.
- U.S. Patent No. 6,242,655 describes a strong acid cation exchange resin as a catalyst.
- the aldehyde content of the ethylene glycol product can be determined by 20 ppm is reduced to below 5 ppm.
- the drawback of the prior method is that the aldehyde content of the ethylene glycol product can only be removed to at most about 2 ppm, and at this time, the ultraviolet light transmittance at 220 nm of the ethylene glycol product has not reached a very desirable value.
- the technical problem to be solved by the present invention is to provide a new method for improving the quality of ethylene glycol products, thereby overcoming the problem of low ultraviolet transmittance of ethylene glycol products existing in the prior art.
- the ethylene glycol product obtained by the method has the advantages of high ultraviolet transmittance and the like.
- the technical scheme adopted by the present invention is as follows: A method for improving the quality of an ethylene glycol product, wherein the ethylene glycol raw material and hydrogen are at a temperature of about 20 to about 280 ° C and a pressure of about 0.1 to about 4.0 MPa. a reaction of about 0.2 to about 100.0 hours, a hydrogen to ethylene glycol molar ratio of about 0.01 to 40:1, through a rotating packed bed reactor containing a solid oxide catalyst, and reacting to obtain ethylene glycol;
- the solid oxide catalyst is selected from at least one of a copper-based, nickel-based, and palladium-based catalyst, and the rotating packed bed reactor has a rotational speed of from about 300 to about 5000 rpm.
- the temperature is from about 30 to about 260 ° C
- the pressure is from about 0.3 to about 3.0 MPa
- the space velocity is from about 1 to about 50.0 hours.
- the molar ratio of hydrogen to ethylene glycol is from about 0.1 to 30: 1.
- the rotating packed bed reactor has a rotational speed in the range of from about 500 to about 3000 rpm.
- the ethylene glycol feedstock is derived from ethylene glycol produced by hydrogenation of oxalate.
- Product The mass concentration of the ethylene glycol starting material is preferably greater than 99%.
- the solid oxide catalyst has a strength ranging from about 60 to about 400 N/cm and a strength preferably ranging from about 100 to about 300 N/cm.
- This strength can be obtained using an organic binder such as polyvinyl alcohol, hydroxypropylmethylcellulose, methylcellulose or hydroxypropylmethylcellulose.
- the solid oxide catalyst obtained from the organic binder can be used at a lower temperature in the above method.
- the solid oxide catalyst may have the following parameters:
- the surface area is from about 10 to about 500 square meters per gram, the pore volume is from about 0.1 to about 1 milliliter per gram, and the average pore diameter is from about 2 to about 13 nanometers.
- the solid oxide catalyst is, for example, a catalyst containing palladium oxide and/or copper oxide and/or nickel oxide.
- the solid oxide catalyst may contain a conventional carrier and optionally a conventional adjuvant.
- the support may for example be a silica, alumina and/or molecular sieve.
- the solid oxide catalyst can be prepared by methods in the art.
- the rotating packed bed reactor may be, for example, a HIGEE-001 type reactor (manufactured by SRIPT).
- the purity of the diol has been 4 ⁇ , but the UV transmittance of the ethylene glycol products at 220nm, 275nm and 350nm still reaches a very good value (the standard of China National Standard Glycol Premium is ethylene glycol).
- the UV transmittance of the products at 220nm, 275nm and 350nm is greater than 75, 95 and 98 respectively. The reason is that trace amounts of trace impurities in the ppm level have a significant effect on the UV transmittance of the product, and these ppm levels Trace impurities are generally difficult to remove by rectification.
- the present inventors have found in the study that copper-based, nickel-based, and/or palladium-based catalysts have high selectivity for removal of trace impurities in ethylene glycol in the presence of hydrogen.
- the reaction process is mainly controlled by diffusion, and the dispersion of hydrogen has a significant effect on the removal effect of impurities. Therefore, the present invention uses a rotary fill.
- the bed can increase the mass transfer coefficient by the geometrical order of the rotating packed bed, greatly enhance the mass transfer process, and finally effectively remove the impurities affecting the ultraviolet transmittance of the product, and significantly improve the quality of the product.
- the ultraviolet light transmittance of the obtained ethylene glycol product at 220 nm is greater than 75, the ultraviolet light transmittance at 275 nm is greater than 95, and the ultraviolet light transmittance at 350 nm is greater than 98, and a good technique is obtained. effect.
- Nickel solid oxide (15% nickel oxide by weight of catalyst, alumina as carrier) is used as catalyst, catalyst strength is 100 N/cm, surface area is 200 m 2 /g, pore volume is 0.31 ml/g, average pore diameter 5 nanometers, using ethylene glycol products obtained by hydrogenation of dimethyl oxalate as raw materials, hydrogen and ethylene glycol raw materials (the purity of ethylene glycol raw materials is 99.8 %, and the ultraviolet transmittance of the raw materials is 2 at 220 nm.
- the obtained ethylene glycol product has a UV light transmittance of 78 at 220 nm, an ultraviolet light transmittance of 95 at 275 nm, and an ultraviolet light transmittance of 100 at 350 nm.
- ethylene is prepared by hydrogenation of dimethyl oxalate.
- the alcohol product is the raw material, and the hydrogen and ethylene glycol raw materials (the purity of the ethylene glycol raw material is 99.8 %, the ultraviolet transmittance of the raw material is 2 at 220 nm, 91 at 275 nm, 95 at 350 nm), and the temperature is 90°.
- the ethylene glycol product obtained after hydrogenation has an ultraviolet light transmittance of 77 at 220 nm, an ultraviolet light transmittance of 96 at 275 nm, and an ultraviolet light transmittance of 100 at 350 nm.
- catalyst strength is 10 10 N/cm
- surface area is 400 m 2 /g
- pore volume is 0.6 ml / g
- average pore diameter is 3 nm
- ethylene glycol obtained by hydrogenation of dimethyl oxalate The product is a raw material, and the hydrogen and ethylene glycol raw materials (the purity of the ethylene glycol raw material is 99.9 %, the ultraviolet transmittance of the raw material is 0 at 220 nm, 90 at 275 nm, 95 at 350 nm), and the temperature is 40.
- the rotating packed bed reactor was rotated at 1000 rpm.
- the ethylene glycol product obtained after hydrogenation has an ultraviolet light transmittance of 79 at 220 nm, an ultraviolet light transmittance of 97 at 275 nm, and an ultraviolet light transmittance of 99 at 350 nm.
- nickel solid oxide as a catalyst (30% nickel oxide by weight of catalyst, ZSM-5 molecular sieve as carrier), the catalyst strength is 210 N/cm, the surface area is 450 m 2 /g, and the pore volume is 0.6 ml/g.
- the average pore diameter is 6 nm, and the ethylene glycol product obtained by hydrogenation of diethyl oxalate is used as a raw material, and the hydrogen and ethylene glycol raw materials (the purity of the ethylene glycol raw material is 99.8 %, and the ultraviolet transmittance of the raw material is 220 nm).
- the catalyst is contacted and the effluent of ethylene glycol is obtained after the reaction; wherein the rotational speed of the rotating packed bed reactor is 2000 rpm.
- the ethylene glycol product obtained after hydrogenation has a UV light transmittance of 78 at 220 nm, an ultraviolet light transmittance of 96 at 275 nm, and an ultraviolet light transmittance of 100 at 350 nm.
- ⁇ Use copper solid oxide as catalyst (20% copper oxide as carrier weight, alumina is supported), catalyst strength is 80N/cm, surface area is 180 m 2 /g, pore volume is 0.4 cc / gram, average The pore size is 4 nm, and the ethylene glycol product obtained by hydrogenating diethyl oxalate is used as a raw material, and the hydrogen and ethylene glycol raw materials (the purity of the ethylene glycol raw material is 99.8 %, The UV transmittance of the material is 10 at 220 nm, 93 at 275 nm, 95 at 350 nm, and at a temperature of 180 ° C, a pressure of 0.5 MPa, and a space velocity of 15 hours.
- the ratio of hydrogen to ethylene glycol is 20:1.
- the effluent of ethylene glycol is obtained by contacting the catalyst by rotating a packed bed reactor under the conditions; wherein the rotational speed of the rotating packed bed reactor is 1000 rpm.
- the ethylene glycol product obtained after hydrogenation has a UV light transmittance of 79 at 220 nm, an ultraviolet light transmittance of 97 at 275 nm, and an ultraviolet light transmittance of 100 at 350 nm.
- catalyst strength is 130 N/cm
- surface area is 250 m 2 /g
- pore volume is 0.6 ml/g
- ethylene glycol product obtained by hydrogenation of dimethyl oxalate as raw material hydrogen and ethylene glycol raw materials
- ethylene glycol raw material purity is 99.8 %
- the ultraviolet transmittance of the raw material is 0 at 220 nm, 90 at 275 nm, 95 at 350 nm, at a temperature of 240 ° C, a pressure of 2.0 MPa, a space velocity of 60 hours, a ratio of hydrogen to ethylene glycol of 30:1, through a rotating packed bed reactor, with the catalyst
- the ethylene glycol effluent is obtained after the reaction; wherein the rotational temperature of the rotating packed bed reactor is 1,500 rpm.
- the ethylene glycol product obtained after hydrogenation has an ultraviolet light transmittance of 80 at 220 nm, an ultraviolet light transmittance of 97 at 275 nm, and an ultraviolet transmittance of 100 at 350 nm.
- catalyst strength is 160 N/cm
- surface area is 80 m 2 /g
- pore volume is 0.2 ml/g
- ethylene glycol product obtained by hydrogenation of dinonyl oxalate as raw material hydrogen and ethylene glycol raw materials
- ethylene glycol raw material purity is 99.8 %
- the ultraviolet transmittance of the raw material is 0 at 220 nm, 90 at 275 nm, 95 at 350 nm, at a temperature of 80 ° C, a pressure of 1.0 MPa, a space velocity of 10 hours, a ratio of hydrogen to ethylene glycol of 10:1, through a rotating packed bed reactor
- the catalyst was contacted, and an ethylene glycol effluent was obtained after the reaction; wherein the rotational speed of the rotating packed bed reactor was 3000 rpm.
- the ethylene glycol product obtained after hydrogenation has an ultraviolet light transmittance of
- Example 8 Palladium and nickel composite solid oxides were used as catalysts (0.12% palladium oxide, 8% nickel oxide, alumina supported), catalyst strength 120 N/cm, surface area 160 m/g, pore volume It is 0.38 ml / gram, the average pore diameter is 5 nm, and the ethylene glycol product obtained by hydrogenating dimethyl oxalate is used as raw material, and the hydrogen and ethylene glycol raw materials (the purity of the ethylene glycol raw material is 99.8 %, the ultraviolet ray of the raw material is transparent).
- the light rate is 10 at 220 nm, 88 at 275 nm, 95 at 350 nm, at a temperature of 80 ° C, a pressure of 0.5 MPa, a space velocity of 15 hr - 1 , and a hydrogen to ethylene glycol ratio of 15:1.
- the effluent of ethylene glycol is obtained by contacting the catalyst by rotating a packed bed reactor; wherein the rotational speed of the rotating packed bed reactor is 1000 rpm.
- the ethylene glycol product obtained after hydrogenation has an ultraviolet light transmittance of 81 at 220 nm, a transmittance of 96 at 275 nm, and an ultraviolet transmittance of 100 at 350 nm.
- the same catalyst, starting materials and reaction conditions as in Example 6 were used except that the reactor was packed in a fixed bed tubular reactor.
- the ethylene glycol product obtained after hydrogenation has a UV light transmittance of 50 at 220 nm, a UV light transmittance of 92 at 275 nm, and an ultraviolet light transmittance of 99 at 350 nm.
- the same catalyst, starting materials and reaction conditions as in Example 7 were used except that the reactor was packed in a fixed bed tubular reactor.
- the ethylene glycol product obtained after hydrogenation has a UV light transmittance of 60 at 220 nm, an ultraviolet light transmittance of 93 at 275 nm, and an ultraviolet light transmittance of 99 at 350 nm. Therefore, it is apparent from the above embodiments that the present invention achieves the technical effects described.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
RU2013143311/04A RU2565589C2 (ru) | 2011-02-25 | 2012-02-24 | Способ улучшения качества продуктов этиленгликоля |
AU2012220220A AU2012220220B2 (en) | 2011-02-25 | 2012-02-24 | Method for improving quality of ethylene glycol product |
US14/000,878 US9051236B2 (en) | 2011-02-25 | 2012-02-24 | Method for improving the quality of ethylene glycol products |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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CN201110045250.3A CN102649687B (zh) | 2011-02-25 | 2011-02-25 | 提高乙二醇产品质量的方法 |
CN201110045250.3 | 2011-02-25 |
Publications (1)
Publication Number | Publication Date |
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WO2012113269A1 true WO2012113269A1 (zh) | 2012-08-30 |
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ID=46691817
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/CN2012/000240 WO2012113269A1 (zh) | 2011-02-25 | 2012-02-24 | 提高乙二醇产品质量的方法 |
Country Status (6)
Country | Link |
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US (1) | US9051236B2 (zh) |
CN (1) | CN102649687B (zh) |
AU (1) | AU2012220220B2 (zh) |
MY (1) | MY162961A (zh) |
RU (1) | RU2565589C2 (zh) |
WO (1) | WO2012113269A1 (zh) |
Cited By (5)
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CN103721717A (zh) * | 2013-12-26 | 2014-04-16 | 上海焦化有限公司 | 一种提高煤基乙二醇产品质量的催化剂及其制备方法 |
US10534308B2 (en) | 2015-03-24 | 2020-01-14 | Mitsubishi Chemical Corporation | Transmission device for a photosensitive drum |
CN112439434A (zh) * | 2019-09-02 | 2021-03-05 | 中国石油化工股份有限公司 | 乙二醇加氢精制剂及其应用 |
CN112439412A (zh) * | 2019-09-02 | 2021-03-05 | 中国石油化工股份有限公司 | 用于乙二醇加氢精制的精制剂及其制备方法 |
CN114478190A (zh) * | 2020-10-27 | 2022-05-13 | 中国石油化工股份有限公司 | 一种乙二醇的精制方法 |
Families Citing this family (6)
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CN104045516B (zh) * | 2013-03-13 | 2016-08-24 | 中国石油化工股份有限公司 | 提高乙二醇产品质量的方法 |
CN104109081B (zh) * | 2013-04-16 | 2016-04-06 | 中国石油化工股份有限公司 | 提高合成气制乙二醇产品质量的方法 |
CN105622348B (zh) * | 2014-11-28 | 2018-06-08 | 中国科学院大连化学物理研究所 | 一种沸点接近的多元醇混合物的分离方法 |
CN110961111B (zh) * | 2019-12-19 | 2022-07-26 | 常州大学 | 一种用于乙二醇加氢精制的负载型催化剂及其制备方法 |
EP4301502A1 (en) * | 2021-03-05 | 2024-01-10 | Scientific Design Company, Inc. | Cycle water treatment process for ethylene epoxidation |
US20230032113A1 (en) * | 2021-07-30 | 2023-02-02 | Armand J. Noel | Solvents, methods, and systems for isolating cannabinoids from plants extracts or from synthetic pathways |
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WO1999058483A1 (en) * | 1998-05-14 | 1999-11-18 | Huntsman Petrochemical Corporation | Improved glycol purification |
CN101058526A (zh) * | 2007-04-11 | 2007-10-24 | 江苏工业学院 | 一种提高乙二醇质量的方法 |
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US4762817A (en) * | 1986-11-03 | 1988-08-09 | Union Carbide Corporation | Aldehyde hydrogenation catalyst |
RU2058285C1 (ru) * | 1993-06-25 | 1996-04-20 | Чебоксарское производственное объединение "Химпром" | Способ получения алкан( c2-c3 )диолов |
US6603048B1 (en) | 1999-10-05 | 2003-08-05 | E. I. Du Pont De Nemours And Company | Process to separate 1,3-propanediol or glycerol, or a mixture thereof from a biological mixture |
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US6770790B1 (en) * | 2003-10-17 | 2004-08-03 | Arco Chemical Technology, L.P. | Purification of tertiary butyl alcohol |
GB0421928D0 (en) * | 2004-10-01 | 2004-11-03 | Davy Process Techn Ltd | Process |
CN100417436C (zh) * | 2005-07-14 | 2008-09-10 | 中国石油化工股份有限公司 | 一种催化选择加氢的方法 |
CN101928201B (zh) * | 2009-06-26 | 2013-04-10 | 上海焦化有限公司 | 一种煤制乙二醇粗产品的提纯工艺 |
-
2011
- 2011-02-25 CN CN201110045250.3A patent/CN102649687B/zh active Active
-
2012
- 2012-02-24 US US14/000,878 patent/US9051236B2/en active Active
- 2012-02-24 RU RU2013143311/04A patent/RU2565589C2/ru active
- 2012-02-24 AU AU2012220220A patent/AU2012220220B2/en active Active
- 2012-02-24 MY MYPI2013701480A patent/MY162961A/en unknown
- 2012-02-24 WO PCT/CN2012/000240 patent/WO2012113269A1/zh active Application Filing
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WO1999058483A1 (en) * | 1998-05-14 | 1999-11-18 | Huntsman Petrochemical Corporation | Improved glycol purification |
CN101058526A (zh) * | 2007-04-11 | 2007-10-24 | 江苏工业学院 | 一种提高乙二醇质量的方法 |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103721717A (zh) * | 2013-12-26 | 2014-04-16 | 上海焦化有限公司 | 一种提高煤基乙二醇产品质量的催化剂及其制备方法 |
CN103721717B (zh) * | 2013-12-26 | 2019-06-25 | 上海华谊能源化工有限公司 | 一种提高煤基乙二醇产品质量的催化剂及其制备方法 |
US10534308B2 (en) | 2015-03-24 | 2020-01-14 | Mitsubishi Chemical Corporation | Transmission device for a photosensitive drum |
CN112439434A (zh) * | 2019-09-02 | 2021-03-05 | 中国石油化工股份有限公司 | 乙二醇加氢精制剂及其应用 |
CN112439412A (zh) * | 2019-09-02 | 2021-03-05 | 中国石油化工股份有限公司 | 用于乙二醇加氢精制的精制剂及其制备方法 |
CN112439434B (zh) * | 2019-09-02 | 2023-08-29 | 中国石油化工股份有限公司 | 乙二醇加氢精制剂及其应用 |
CN114478190A (zh) * | 2020-10-27 | 2022-05-13 | 中国石油化工股份有限公司 | 一种乙二醇的精制方法 |
CN114478190B (zh) * | 2020-10-27 | 2024-03-05 | 中国石油化工股份有限公司 | 一种乙二醇的精制方法 |
Also Published As
Publication number | Publication date |
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MY162961A (en) | 2017-07-31 |
CN102649687A (zh) | 2012-08-29 |
US20130331618A1 (en) | 2013-12-12 |
AU2012220220A1 (en) | 2013-09-05 |
RU2013143311A (ru) | 2015-04-10 |
CN102649687B (zh) | 2014-11-26 |
AU2012220220B2 (en) | 2016-08-18 |
US9051236B2 (en) | 2015-06-09 |
RU2565589C2 (ru) | 2015-10-20 |
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